Synthetic approaches are widely employed in the emerging research field of systems and synthetic biology, to learn the living organisms in a physical and systematic manner, such as, cellular dynamics and network interactions. Synthetic gene circuits potentially offer the insights into nature’s underlying design principles (Hasty et al, 2002), and genetic reconstructions will give better understanding of naturally occurring functions (Sprinzak and Elowitz, 2005). Technical improvements in synthetic biology will provide not only engineering novelty for applications in biotechnology (McDaniel and Weiss, 2005) but also the fundamental understanding of living systems.
It is well-known that a library of the parts comprised in the gene circuits, which can be found in MIT Parts Registry (http://parts.mit.edu/), provides a variety for genetic reconstruction. As well, a new born organization (http://biobricks.org/) provides a platform (BioBrickTM parts) for scientists and engineers to work together. Current pioneer studies provided the successful examples of synthetic circuits working in the living cells, such as, the mutual inhibitory circuits functionally constructed in bacterial cells (Gardner et al, 2000), and with newly introduced biological functions (Kashiwagi et al, 2006). However, the reported cases generally do not include the vast majority of many failures. After defining a conceptual design as specifying how individual components are connected to accomplish the desired function, the next step is constructing the well-designed foreign circuit in living cells. So far, the strategies for construction of synthetic gene circuits are more of an art form than a well-established engineering discipline, mostly, in a “Plug and Play” manner (Haseltine and Arnold, 2007).
Carriers (vector) used for genetic construction are commonly limited in the plasmid, due to the advantageous of its efficiency and easy manipulation. Successful constructions have been reported to mimic a toggle switch in bacterial cells (Gardner et al, 2000), to build a synthetic predator-prey ecosystem (Balagadde et al, 2008), to address the dynamical property of positive feedback system (Maeda and Sano, 2006), to study the behaviour of the synthetic circuit under complex conditions: unregulated, repressed, activated, simultaneously repressed and activated (Guido et al, 2006). However, noise due to the copy number variation in plasmids is inevitable. As know, copy number variation is an important and widespread component within and between cell populations. For example, CNV can cause statistically significant changes in concentrations of RNA associated with growth rate changes in bacteria (Klappenbach et al, 2000; Stevenson and Schmidt, 2004); as well as, small-scale copy number variation can cause a dramatic, nonlinear change in gene expression from the theoretical study on various genetic modules (network motifs) (Mileyko et al, 2008). Thus, low-copy plasmids are utilized for generation of cellular function in the studies of demonstrating that negative auto-regulation speeds the response times of transcription networks (Rosenfeld et al, 2002), identifying heuristic rules for programming gene expression with combinatorial promoters (Cox et al, 2007), studying the biological networks and produce diverse phenotypes (Guet et al, 2002), etc. As well, combination of low-copy plasmid and genome has been applied to analyze the multistablity in lactose operon in bacterial (Ozbudak et al, 2004), to evaluate the fluctuation in gene regulation at the single cell level (Rosenfeld et al, 2005), and to study noise propagation (Pedraza and van Oudenaarden, 2005), and so on. Nevertheless, neither controlling the copy number of plasmid in a living cell nor keeping a constant copy number of plasmid in a growing cell population is easy.
Difficulties in synthetic approaches of genetic constructions are faced, in particular, as the fact that a stable construction is essential for steady phenotypic quantification. Practical methodology is required for the stable maintenance of the synthetic gene circuits in growing cells. As the genome is the most stable genetic circuit in living cells, insertion synthetic circuit into the genome will promise a best solution. Short fragment genome recombination of a reporter gene is widely applied, particularly, such as, the accurate prediction of the behaviour of gene circuits from component properties (Rosenfeld et al, 2007), and the study on intrinsic and extrinsic noise in a single cell level (Elowitz et al, 2002). It is becoming aware of the importance of genome integration of the synthetic gene networks.
Though the single copy of genome is the best choice for carrying the synthetic circuit stable along with the cell division and propagation, building a complex synthetic circuit, commonly comprised of a few genetic parts, into genome is not an easy job due to the flowing reasons. Inducing these parts into the genome one by one is time consuming, and the frequently repeated genomic construction process can potentially result in unexpected mutagenesis or stress-induced genomic recombination. The modified method introduced here reduces the frequency of recombination, and provides a time-saving approach for efficient synthetic construction on the bacterial genome. The availability of long insertions allows the easy artificial reconstruction of complicated networks on the genome. The examples of synthetic circuits constructing in Escherichia coli cells using the refined methods are described in detail. An assortment of synthetic circuits integrated into the genome working as design principles are shown. The switch-like response of the synthetic circuit sensitive to nutritional conditions is specially presented. Constructing synthetic gene circuits integrated in bacterial genome is to form a stable built-in artificial structure, and provides a powerful tool for the studies not only on the field of synthetic and systems biology based on bacteria but also on the applications potential for genetic engineering to achieve metabolic reconstruction.
2. Methodology: Genome-integration of foreign DNA sequences
As the classic methods for genome recombination, a number of general allele replacement methods have been used to inactivate bacterial chromosomal genes (Dabert and Smith, 1997; Kato et al, 1998; Link et al, 1997; Posfai et al, 1999). These methods all require creating the gene disruption on a suitable plasmid before recombining it onto the chromosome, leading to its complexity in the methodology. A relatively simple method was developed by Wanner’s group, a simple and highly efficient method to disrupt chromosomal genes in Escherichia coli in which PCR primers provide the homology to the targeted genes (Datsenko and Wanner, 2000). The procedure is based on the Red system that promotes a greatly enhanced rate of recombination over that exhibited by recBC, sbcB, or recD mutants when using linear DNA.
Elegant applications of Wanner’s method have been reported, such as, the construction of single-gene knock-out mutants (Baba et al, 2006), construction of targeted single copy of lac fusions (Ellermeier et al, 2002), produce insertion alleles for about 2,000 genes systematic mutagenesis of Escherichia coli genome (Kang et al, 2004). Because of the limitation on the insertion length, the optimization on transformation procedure was performed to produce recombinant prophages carrying antibiotic resistance genes (Serra-Moreno et al, 2006). Wanner’s method is very efficient on deletion mutation, even for quite long genome segments, whereas, insertion is limited within 2-3 Kbs technically. The requirement on constructing complicated networks is facing to the technical problem on the length limitation.
The methodology of genetic construction was recently published as the research article on a new protocol for more efficient integration of larger genetic circuits into the Escherichia coli chromosome. Complex synthetic circuits are commonly comprised of a few genetic parts. Inducing these parts into the genome one by one is time consuming, and the frequently repeated genomic construction process can potentially result in unexpected mutagenesis or stress-induced genomic recombination. The refined procedure introduced here shows the availability of the efficient artificial reconstruction of complex networks on the Escherichia coli genome, and provides a powerful tool for complex studies and analysis in synthetic and systems biology. Comparison between the genome integrated and the plasmid incorporated genes, reduced cell-to-cell variation was clearly observed in genome format. The method demonstrated that the integrated circuits show more stable gene expression than those on plasmids and so we feel this technique is an essential one for microbiologists to use.
2.1. Refined method
The method has been modified including medium, temperature, transformation, and selection, as described elsewhere (Ying et al, 2010). The synthetic sequences need to be wholly constructed on a plasmid in advance. Following PCR amplification and purification of the linear target sequence, transformation (electroporation) for genome replacement is performed, to introduce it into competent cells. To distinguish genomic recombinants from the original plasmid carriers, the target synthetic sequence encodes a different antibiotic resistant gene from the original plasmid. False transformants (i.e., transformed colony) carrying the plasmid grow on both antibiotic plates; genomic recombinants grow only on the plate carrying the antibiotic whose resistant gene is encoded in the circuit, but not the one encoded in the plasmid. Dual antibiotics selection for positive transformants reduces the labour and cost of large-scale screening, and uncovers a high ratio of positive candidates on the colony PCR check. The steps of the refined method are described as follows, along with the schematic illustration of the process (Figure 1).
Construction of the synthetic sequence on a plasmid (often containing an AmpR gene).
PCR amplification of the target foreign DNA sequence, with the homogenous region corresponding to the recombination site.
Clean-up (buffer exchange or gel extraction) using commercial kits.
Digestion by the enzyme DpnI at 37˚C for 2 h to remove the trace amount of the original plasmid.
Clean-up and condensation of the target sequence. Any commercial kit is convenient.
Transformation to the host strain containing the plasmid of pKD46, encoding the recombinase. Electroporation is crucial.
Culturing in the rich medium (SOC) with 1 mM of arabinose, at 37˚C for 2 h. Quiet incubation often increases the efficiency of transformation.
Plating for antibiotic selection, incubation overnight at 37˚C. Once using a slow growth strain, the additional incubation time is required.
Strike the single colonies onto two plates, each with a different antibiotic, and incubate overnight at 37˚C.
Selection based on the difference of the clones between the two plates: positive candidates exhibited fast growth on the GeneR (the antibiotics resistant gene different from AmpR) plate, and slow or no growth on the AmpR plate. This dual antibiotics screening on the plates promoted the final positive selection by colony PCR.
Colony PCR for final confirmation. This step is essential to make sure that no unexpected recombination occurred in genome, particularly repeated homologous recombination have been performed.
2.2. High efficiency of recombination
Synthetic DNA sequences of various lengths (1 ― 10 Kbs) have been inserted into the different sites on genome, such as, intC, argG, glnA, leuB, ilvE, hisC and galK. Comparatively short insertions result in accurate genome replacement. In contrast, longer insertions generally lead to fewer transformants and a worse outcome (i.e., fewer positive colonies); nevertheless, usually there are still sufficient transformants for further selection (Table 1). Genome location (gene site) dependent efficiency of homologous recombination was noticed (unpublished data). The site of galK always gave the best score of successful recombination, regardless of the length of inserted sequences. The efficiency of successful recombination, based on the positive ratio of the colony PCR, depended on the insertion length. Previous studies provide myriad examples of short DNA fragment recombinations (Elowitz et al, 2002), but none of long ones. The ability of this methodology to successfully recombine a foreign DNA fragment of 9 to 10 Kbs indicates that it is possible to construct a complex synthetic gene circuit of a considerable length onto the bacterial genome.
In addition, the homologous sequences of various lengths have been evaluated for the transformation efficiency at the identical genome location. In general, a 100-bp overlap, which can be easily generated by PCR amplification, could enable reasonably high genome recombination efficiency. Thought longer homologous sequences are supposed to give higher recombination efficiency, our test showed that length dependency was only present when the homologous sequence ranged from 50 to 150 bps, as an overlap of 300 to 500 bps decreased the number of transformants (Ying et al, 2010). We assume that the accessibility of the secondary structure, caused by the complex conformation of genome, for annealing possibly plays a role in successful recombination. According to the reported studies, genome integration has been generally carried out for 1 or 2 genes for each recombination step. If a relatively large fragment comprising 4 to 8 genes, four cycles of genome recombination procedure are needed. The reduced repetition of homologous recombination procedure of this refined protocol allows long DNA segments exchange at once. It greatly saves time and labour, and is supposed to contribute to the microbiological engineering.
2.3. Reduced cell-to-cell variation
Copy number variation in genetic materials can cause large variation within and between cell populations. As reported, it caused significant changes in RNA concentrations associated with growth rate changes (Klappenbach et al, 2000; Stevenson et al, 2004), as well as dramatic differences in gene expression compared to theory in various genetic modules (network motifs) (Mileyko et al, 2008). It is why combination of low-copy plasmids and genomes is currently applied in the studies on fluctuations in living cells (Ozbudak et al, 2004; Rosenfeld et al, 2005).
The relation between the copy number of the plasmid and the cell-to-cell variation in gene expression has been evaluated by an assortment of experiments using the flow cytometry, as previously reported (Ito et al, 2009). The results showed that the copy number of the plasmid was correlated to the protein abundance, which indicated that the variable in DNA copy number contributed to the cell-to-cell variation in gene expression. The copy number issue is important to be considered, when discussing the property of the target gene and its expression fluctuation. Genomic recombination seems to be the best choice for the studies on biological noise and phenotypic fluctuation, as the genome is a stable carrier of the constant copy number.
The comparison between the plasmid and the genome clearly verified this statement. Identical synthetic sequence, comprising a reporter gene gfp (green fluorescence protein, GFP) and an antibiotic resistant gene kan R , has been transformed into the host Escherichia coli cells, either in a low-copy plasmid (~ 20 copies per cell) or onto the genome. Once both cell types were induced to display similar green fluorescent intensities (i.e., the same averaged concentration of GFP), the variance of the cellular GFP concentration obtained from plasmid carriers was much larger than that from genomic carriers (Ying et al, 2010). It demonstrates that the variety of gene expression levels among the cells carrying the synthetic sequence in plasmid format is much larger than that in the genomic format. Using a very low-copy plasmid (< 5 copies per cell) reduced the cell-to-cell variation but still showed larger variance than the genome format (unpublished data). It greatly suggests that it is noise in the gene copy number that increases the variation in a genetically identical population. In addition, less heterogeneous in the transformant phenotypes and longer generations were often observed in genome-integrated carriers than those of plasmid insertion (personal communication). Taken together, construction of a synthetic gene circuit on the genome will greatly improve the stability of the genetic structure itself and reduce the biological noise from copy number variation.
3. Applications: Synthetic gene circuits work as design principles
An applicable protocol for solid and efficient genome recombination is described above. An assortment of well-designed synthetic circuits built-in Escherichia coli cells are going to be introduced as successful applications. Precise reconstruction of synthetic gene circuits to mimic gene expression and regulation is generally employed in a plasmid with a chromosomal reporter gene (Blake et al). Using the modified method, we successful integrated a variety of gene circuits into the bacterial genome. First of all, a relatively long genetic loop of mutual inhibitory structure displayed a strong hysteric expression pattern was successfully constructed, which was assumed to be resulted from the decreased fluctuation due to the genome recombination. Applying the mutual inhibitory design, a bistable dual function genetic switch was built in the genome. Selective expression of the genome integrated genetic switch sensitive to the environmental transition was clearly observed, which suggested that the synthetic circuits could show physiological activity in living cells and play an important role in population adaptation.
3.1. Mutual inhibitory construct behaved as design principles
Mutual inhibitory structure has been successfully constructed in bacterial cells on the plasmids (Gardner et al, 2000; Kashiwagi et al, 2006), and the pretty work of this structure in genome format was firstly reported using the refined method (Ying et al, 2010). As shown in Figure 2A, the mutual inhibitory structure, which was integrated into the genome and showed the expected features, was finally acquired using the method described here. The Escherichia coli DH1 cells were used as hosts for the construct. To prevent disturbance of the expression from the promoter Plac by the endogenous level of LacI protein, the native lacI gene and the related genes lacY and lacZ were deleted from the genome. The reporter genes, gfp and rfp, were employed as two different visible phenotypes and were used for quantitative evaluation of the protein levels of the two repressor proteins, TetR and LacI. The two antibiotic resistant genes were used as selection markers during genetic construction. According to the design principle, when the two expression units (i.e., gfp-lacI-kan R and rfp-tetR-cat R ), which are regulated by the promoters Plac and Ptet, respectively, are expressed, they will inhibit each other, and the cells will show a “red” or “green” phenotype. The gfp-lacI-kan R unit is highly induced (“green” phenotype) when the chemical inducer, doxycycline (Dox), is added. Similarly, the rfp-tetR-cat R unit is greatly induced (“red” phenotype) by isopropyl β-D-1-thiogalactopyranoside (IPTG).
The engineered Escherichia coli cells carrying this mutual inhibitory structure (Figure 2A) displayed either green or red fluorescent intensity (Figure 2B), representing the two discrete phenotypes of highly induced expression of either unit. As known, the positive feedback structure could accelerate the expression of any of the two expression units occasionally showing slightly higher expression level, while the mutual inhibitory structure would suppress expression of the other unit, leading to a fixation effect of the expressed unit (Gardner et al, 2000; Kashiwagi et al, 2006; Ozbudak et al, 2004). The discrete expression of the two units verified the bistable nature, involved in the mutual inhibitory structure, as designed features.
Following preliminary incubation in a doxycycline-free or doxycycline-supplemented (40 nM) medium, Escherichia coli cells carrying the mutual inhibitory structure were cultured in various concentrations of doxycycline (i.e., 0, 5, 10, 15, 20, 30 and 40 nM) to induce the expression of gfp-lacI-kan R , the “green” unit. Due to the different initial states, that is, the “green” or “red” induced expression level, the gfp expression levels varied even under the same condition, for instance, in the presence of 5 nM doxycycline, cells with high expression of the “red” unit at preincubation (doxycycline-free condition) showed an induced expression of rfp after incubation (Figure 3, upper panel), while those with high expression of “green” unit in preincubation (doxycycline-supplemented condition) showed an induced expression of gfp after incubation (Figure 3, bottom panel). The hysteresis in gene expression was clearly observed in the engineered Escherichia coli cells, under the inductions of 5 ― 15 nM doxycycline, and kept for several days undergoing serial transfer, equal to approximate 30 to 50 generations. It indicated that the applicable synthetic approach of building genome integrated gene circuits successfully presenting the designed principles.
The success of the synthetic design was due to the easy genomic construction method. Construction of a simple toggle switch on a plasmid and transformation into bacterial cells was previously reported (Gardner et al, 2000). A genomic version of the similar toggle switch is introduced here. It could be steadily maintained along with propagation and cell division. Note that, to optimize this structure (i.e., for strong hysteresis of gene expression), the “green” unit (i.e., gfp-lacI-kan R ) was fixed and the regulatory region of the “red” one (i.e., rfp-tetR-cat R ) was flexible, by using various operators or promoters. As differences in the sequence of promoters and the number of operators could strongly influence the binding affinity of the repressor proteins, regardless of the identical promoter, the operator sequences have been adjusted to amend the expression level of the repressors. The promoters and operators have been optimized for the enhanced binding affinity with the repressors, strong hysteresis (memory effect) was clearly observed in this construction. Owing to the greatly reduced copy number of the genome integrated synthetic construct, the changes in binding affinity of operator and repressor were clearly observed. The final construct of the satisfying promoter and operator sequences was decided by means of the “Plug and Play” strategy (Haseltine et al, 2007). Thus, optimization of the genetic construct in genome becomes practical, as the modification of the method reduces the steps and increases the efficiency of genome recombination.
3.2. Synthetic switch sensitive to environmental transitions
An assortment of synthetic circuits of varied genetic designs has been successfully constructed into the Escherichia coli genome (Kashiwagi et al, 2009; Ying et al, 2010). Experimental investigation demonstrated that these synthetic circuits were functional in living cells and could survive cells from starvation (Tsuru et al, 2011; Shimizu et al, in revision). Among these constructs, a relatively complex circuit of mutual inhibitory structure (Matsumoto et al, 2011) is introduced here.
3.2.1. Design principles
As described, bistability can be easily introduced into the genetic design of the synthetic circuit to produce two discrete stable states, “red” and “green”, as shown in Figure 2B. Once the biological functions, for instance, which are crucial for cell growth, are introduced to the synthetic circuit, the two stable states will represent two phenotypes of physiological activities. For instance, two additional genes, geneA and geneB, can be inserted into the two expression units, “red” and “green”, as shown in Figure 4. The geneA and geneB encode the proteins (e.g., enzymes) that catalyze the biological reactions promoting the two independent physiological pathways (Figure 4, Function A and Function B), respectively. Switching between the two expression units is supposed to have selective activation of the two pathways, resulting in growth recovery of cell population and/or causing improved production of target proteins.
Such synthetic gene circuit was finally designed as described elsewhere (Matsumoto et al, 2011) and constructed as follows (Figure 4 and Figure 5). The two expression units, “red” and “green”, representing a dual-function synthetic switch, were built in the Escherichia coli genome by homologous recombination as described in 2.1. The “red” unit contained three genes, rfp, tetR and leuB, encoding a red fluorescent protein (RFP), a repressor protein (i.e., TetR) for blocking expression of the “green” unit (the promoter Ptet) and an enzyme contributing to leucine biosynthesis, respectively. The “green” unit consisted of three genes, gfp, lacI and hisC, encoding a green fluorescent protein (GFP), a repressor protein (i.e., LacI) inhibiting expression of the “red” unit (the promoter Plac) and an enzyme involved in histidine biosynthesis, respectively. That is, the geneA and geneB were replaced by leuB and hisC, and leucine and histidine biosynthesis represented the Function A and B, respectively (Figure 4). By the way, to oblige the cells to use the genes, hisC and leuB, within the synthetic switch, the native regulation of Leu and His operons was disturbed by removing leuB and hisC from their native chromosomal locations. Thus, the expression of leuB and hisC only inside the “red” and “green” units were reported by the red and green fluorescence, respectively. Thus, a synthetic switch based on a mutual inhibitory structure showing two discrete physiological states, the induced leucine (red) and histidine (green) productions, was constructed as designed (details in Matsumoto et al, 2011).
Rewiring of the stress-stringent genes (i.e., leuB and hisC) to the synthetic circuit allows us not only to investigate the unknown survival strategy in living systems but also to search the possibility of metabolism reconstitution. As genome recombination promises a stable genetic carrier, this synthetic dual-function circuit can be applied to mimic cellular behaviour. According to the design principle, the Escherichia coli cells carrying this synthetic switch are able to show two different phenotypes, “red” and “green”, representing the induced expression of leuB and hisC, and related to two physiological functions, i.e., leucine and histidine biosynthesis, respectively (Figure 5). Bistability, resulting from the mutual inhibitory structure, was assumed to confer the “memory effect” on the cells carrying this structure, as shown in Figure 3, where the same promoter and repressor cassette is used. That is, the cells are thought to be able to show two distinct phenotypes under identical culture conditions due to the diverse histories (induction) of gene expression.
Here, two diverse biological functions leucine and histidine biosynthesis are designed, both of which result in a fitness recovery depending on the external conditions (Figure 5). For instance, it is the cells only showing an induced expression level of the “red” unit, which contacting the gene leuB essential for leucine biosynthesis that could survive under leucine-depleted conditions (i.e., Condition A). In general, Escherichia coli cells use the Leu operon and His operon to respond to starvation (Keller and Calvo, 1979; Searles et al, 1983; Wessler and Calvo, 1981). Depletion of leucine will lead to the induced expression of structural genes in the Leu operon; similarly, histidine depletion will cause an increase in expression of proteins encoded within the His operon (Henkin and Yanofsky, 2002; Keller et al, 1979). leuB and hisC, which are located within the Leu and His operons (Gama-Castro et al, 2008), are responsible for leucine and histidine biosynthesis, respectively. Rewiring these stringent starvation genes to the synthetic circuit not only introduces physiological activities to the synthetic design but also disturbs the original native regulation.
3.2.2. Experimental investigation
Firstly, whether the constructed synthetic circuit was functional was examined. The addition of IPTG induced the expression of the “red” unit that comprising leuB greatly improved the cell growth under the leucine-depleted conditions; similarly, the addition of doxycycline (Dox) induced the expression of hisC within the “green” unit, and allowed the cells to grow in histidine-depleted conditions (Table 2). Obviously, the selective full induction of the two expression units enabled the cells to grow under starved conditions. These results verified the following points: 1) the rewired genes, leuB and hisC, were biologically active, regardless of the chromosomal replacement; 2) the repressor-promoter interactions involved in the mutual inhibitory structure were strong; 3) the synthetic circuit was genetically stable and functional in the living cells.
Subsequently, whether the synthetic circuit comprised of the rewired genes can be used by the Escherichia coli cells as a functional genetic switch in response to environmental transition was investigated. Under the hysteretic conditions, exponentially growing cells were transferred to the fresh media without the essential amino acid, leucine or histidine, for growth. Temporal changes in population dynamics were analyzed using flow cytometry, as described somewhere else (Matsumoto et al, in submission). When the “red” cell population of repressed expression of hisC was transferred to histidine-free conditions, the composition of the cell population changed gradually. More and more “green” cells of induced expression of hisC were born within the population, resulted in the population transition from “red” to “green” (Figure 6, left). Similarly, once the “green” cell population of repressed expression of leuB was transferred to leucine-free conditions, the “red” cells of induced expression of leuB were born and the fast growth allowed the “red” cells to take over the whole population, leading to the distribution shift from “green” to “red” (Figure 6, right). Note that in the rich medium, both “red” and “green” populations kept their distributions as initial expression level. Taken together, the Escherichia coli cells carrying this synthetic circuit formed the new population in accordance with the nutritional status.
Furthermore, the relation between cell growth and expression of the synthetic circuit was evaluated. The temporal trajectory of the relation between cell growth and relative expression level in the cell population showed that the growth rate decreased significantly under conditions of leucine or histidine depletion but recovered gradually, accompanied by a gradual increase in leuB (“red” unit) or hisC (“green” unit) expression level. The growth recovery and population transition due to histidine depletion were faster than those due to leucine depletion. The “green” unit (hisC) was much easier to induce than the “red” unit (leuB), possibly due to slight leakage of gene expression from Ptet, diverse essentiality in amino acid requirement, or as yet unknown synchronised expression changes in other related genes, etc. Further applications using other genes and amino acids are required to determine the universality of the capacity of the synthetic circuit to respond to external perturbations and to function as genetic switch sensitive to surroundings.
The experiments demonstrated that bacterial cells carrying this synthetic circuit formed diverse populations in response to the nutritional conditions and survived under conditions of nutrient depletion. A genome-integrated dual-function synthetic circuit sensitive to an environmental transition was successfully acquired. It strongly suggested that the synthetic design of proto-operons sensitive to external perturbations is practical for native cells. In summary, the method of genetic engineering and the application studies introduced here provides an efficient constructive approach for the studies or analysis in bacterial systems biology. Here, the genes involved in physiological functions responsive to external changes are introduced into the two expression units, the selective expression of the two units in cells can be considered a synthetic operon contributing to survival and/or adaptation.
A modified method for the integration of complicated genetic circuits into the Escherichia coli genome is introduced. The methodology provides an efficient synthetic approach for the dynamic and stochastic study of genetic networks. Linear artificial sequences as long as ~ 9 Kbps can be easily integrated into the bacterial genome at one time. The applications clearly showed accurate phenotypic behavior of the genome-integrated synthetic gene circuits corresponding to the design principle, which confirmed that the improved method allows the efficient construction of a single copy of a complicated genetic circuit in cells. As the genome recombination generally minimizes the copy number noise in the genetic circuit, it allows the precise design and interpretation of the cellular network. The availability of long-fragment insertions allows the easy reconstruction of complicated networks on the genome, and provides a powerful tool for synthetic and systems biology. Furthermore, the Escherichia coli cells carrying the synthetic circuit showed selective expression pattern in accordance with the environmental conditions, demonstrated the successful application of the genome-integrated synthetic circuit in cells. The applications owing to the simplified protocol demonstrated that the synthetic construct in the genome could be physiologically functional and sensitive to environmental transition. Synthetic approaches not only leads to the technical evolution for industrial use, but also can be employed to observe novel phenomena in living organisms. Further applications and improvement may bring us the completely synthetic genome functionally works in protocells.
We thank Natsuko Yamawaki, Junko Asada and Natsue Sakata for technical assistance, and the group members for fruitful discussion. This work was partially supported by Grants-in-Aid for Challenging Exploratory Research 22657059 (to BWY) and the “Global COE (Centers of Excellence) program” of the Ministry of Education, Culture, Sports, Science and Technology, Japan.